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Nitrogen-stimulated orotic acid synthesis and nucleotide imbalance
Orotic acid, first discovered in ruminant milk, is an intermediate in the pyrimidine biosynthesis pathway of animal cells. Its synthesis is initiated by the formation of carbamoyl phosphate (CP) in the cytoplasm, with ammonia derived from glutamine. Ureotelic species also form CP in the first step o...
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Published in: | Cancer research (Baltimore) 1992-04, Vol.52 (7), p.2082s-2084s |
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description | Orotic acid, first discovered in ruminant milk, is an intermediate in the pyrimidine biosynthesis pathway of animal cells. Its synthesis is initiated by the formation of carbamoyl phosphate (CP) in the cytoplasm, with ammonia derived from glutamine. Ureotelic species also form CP in the first step of urea synthesis in liver mitochondria. For that, ammonia is derived from tissue fluid. When there is insufficient capacity for detoxifying the load of ammonia presented for urea synthesis, CP leaves the mitochondria and enters the pyrimidine pathway, where orotic acid biosynthesis is stimulated, orotic acid excretion in urine then increases. Orotic acid synthesis is abnormally high with hereditary deficiencies of urea-cycle enzymes or uridine monophosphate synthase. It is also elevated by ammonia intoxication and during feeding of diets high in protein, high in lysine with respect to arginine, or deficient in arginine, ornithine, and citrulline. Rats fed 1% orotic acid or diets deficient in urea-cycle amino acids develop fatty livers, which has not been demonstrated in other species. Humans consuming 6 g of orotic acid daily have not shown adverse effects. Rats fed 1% orotic acid or arginine-deficient diets also showed more and larger foci positive for gamma-glutamyl transpeptidase and more liver tumors after administration of carcinogens and partial hepatectomy. Orotic acid feeding was also associated with the tendency for development of larger mammary tumors induced by chemical carcinogens in rats and with development of urinary bladder calculi containing high concentrations of orotic acid in mice. Conditions that raise tissue orotic acid change purine-pyrimidine ratios. It is unknown whether tissue orotate concentrations play a role in the recently observed enhanced proliferation of cells in the colon of rats fed high-protein, high-fat diets or in the promotion of chemically induced colon cancer by intrarectal administration of ammonium acetate. |
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J</creatorcontrib><description>Orotic acid, first discovered in ruminant milk, is an intermediate in the pyrimidine biosynthesis pathway of animal cells. Its synthesis is initiated by the formation of carbamoyl phosphate (CP) in the cytoplasm, with ammonia derived from glutamine. Ureotelic species also form CP in the first step of urea synthesis in liver mitochondria. For that, ammonia is derived from tissue fluid. When there is insufficient capacity for detoxifying the load of ammonia presented for urea synthesis, CP leaves the mitochondria and enters the pyrimidine pathway, where orotic acid biosynthesis is stimulated, orotic acid excretion in urine then increases. Orotic acid synthesis is abnormally high with hereditary deficiencies of urea-cycle enzymes or uridine monophosphate synthase. It is also elevated by ammonia intoxication and during feeding of diets high in protein, high in lysine with respect to arginine, or deficient in arginine, ornithine, and citrulline. Rats fed 1% orotic acid or diets deficient in urea-cycle amino acids develop fatty livers, which has not been demonstrated in other species. Humans consuming 6 g of orotic acid daily have not shown adverse effects. Rats fed 1% orotic acid or arginine-deficient diets also showed more and larger foci positive for gamma-glutamyl transpeptidase and more liver tumors after administration of carcinogens and partial hepatectomy. Orotic acid feeding was also associated with the tendency for development of larger mammary tumors induced by chemical carcinogens in rats and with development of urinary bladder calculi containing high concentrations of orotic acid in mice. Conditions that raise tissue orotic acid change purine-pyrimidine ratios. It is unknown whether tissue orotate concentrations play a role in the recently observed enhanced proliferation of cells in the colon of rats fed high-protein, high-fat diets or in the promotion of chemically induced colon cancer by intrarectal administration of ammonium acetate.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 1544144</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Ammonia - metabolism ; Animals ; Biological and medical sciences ; Carbamyl Phosphate - metabolism ; Carcinogenesis, carcinogens and anticarcinogens ; Cattle ; Chemical agents ; Humans ; Liver Neoplasms - chemically induced ; Medical sciences ; Milk - metabolism ; Orotic Acid - metabolism ; Orotic Acid - pharmacology ; Orotic Acid - urine ; Pyrimidines - biosynthesis ; Rats ; Triglycerides - metabolism ; Tumors ; Urea - metabolism</subject><ispartof>Cancer research (Baltimore), 1992-04, Vol.52 (7), p.2082s-2084s</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5271091$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1544144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>VISEK, W. J</creatorcontrib><title>Nitrogen-stimulated orotic acid synthesis and nucleotide imbalance</title><title>Cancer research (Baltimore)</title><addtitle>Cancer Res</addtitle><description>Orotic acid, first discovered in ruminant milk, is an intermediate in the pyrimidine biosynthesis pathway of animal cells. Its synthesis is initiated by the formation of carbamoyl phosphate (CP) in the cytoplasm, with ammonia derived from glutamine. Ureotelic species also form CP in the first step of urea synthesis in liver mitochondria. For that, ammonia is derived from tissue fluid. When there is insufficient capacity for detoxifying the load of ammonia presented for urea synthesis, CP leaves the mitochondria and enters the pyrimidine pathway, where orotic acid biosynthesis is stimulated, orotic acid excretion in urine then increases. Orotic acid synthesis is abnormally high with hereditary deficiencies of urea-cycle enzymes or uridine monophosphate synthase. It is also elevated by ammonia intoxication and during feeding of diets high in protein, high in lysine with respect to arginine, or deficient in arginine, ornithine, and citrulline. Rats fed 1% orotic acid or diets deficient in urea-cycle amino acids develop fatty livers, which has not been demonstrated in other species. Humans consuming 6 g of orotic acid daily have not shown adverse effects. Rats fed 1% orotic acid or arginine-deficient diets also showed more and larger foci positive for gamma-glutamyl transpeptidase and more liver tumors after administration of carcinogens and partial hepatectomy. Orotic acid feeding was also associated with the tendency for development of larger mammary tumors induced by chemical carcinogens in rats and with development of urinary bladder calculi containing high concentrations of orotic acid in mice. Conditions that raise tissue orotic acid change purine-pyrimidine ratios. It is unknown whether tissue orotate concentrations play a role in the recently observed enhanced proliferation of cells in the colon of rats fed high-protein, high-fat diets or in the promotion of chemically induced colon cancer by intrarectal administration of ammonium acetate.</description><subject>Ammonia - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Carbamyl Phosphate - metabolism</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>Cattle</subject><subject>Chemical agents</subject><subject>Humans</subject><subject>Liver Neoplasms - chemically induced</subject><subject>Medical sciences</subject><subject>Milk - metabolism</subject><subject>Orotic Acid - metabolism</subject><subject>Orotic Acid - pharmacology</subject><subject>Orotic Acid - urine</subject><subject>Pyrimidines - biosynthesis</subject><subject>Rats</subject><subject>Triglycerides - metabolism</subject><subject>Tumors</subject><subject>Urea - metabolism</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNo9j0tLxDAUhYMo4zj6E4Qs3BbyuGnapQ6-YNCNrofb5EYjfdGki_n3FiyuDofvcDjnjG2l0VVhAcw52wohqsKAVZfsKqWfxRopzIZtpAGQAFv28BbzNHxRX6Qcu7nFTJ4P05Cj4-ii5-nU529KMXHsPe9n19ICPfHYNdhi7-iaXQRsE92sumOfT48f-5fi8P78ur8_FKPSJhdaiqo06EppQaB11qLXVBpFDQlVegIUZVNDQwGkCgIp1KA8-MpoQAx6x27_ese56cgfxyl2OJ2O65eF360ck8M2TMu4mP5jRlkpaql_AZpiU8Q</recordid><startdate>19920401</startdate><enddate>19920401</enddate><creator>VISEK, W. J</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19920401</creationdate><title>Nitrogen-stimulated orotic acid synthesis and nucleotide imbalance</title><author>VISEK, W. J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p235t-310865ac61740a7c77ad3e652ebe026de4a06b94bef412f0aef942d4d8534aaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Ammonia - metabolism</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Carbamyl Phosphate - metabolism</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>Cattle</topic><topic>Chemical agents</topic><topic>Humans</topic><topic>Liver Neoplasms - chemically induced</topic><topic>Medical sciences</topic><topic>Milk - metabolism</topic><topic>Orotic Acid - metabolism</topic><topic>Orotic Acid - pharmacology</topic><topic>Orotic Acid - urine</topic><topic>Pyrimidines - biosynthesis</topic><topic>Rats</topic><topic>Triglycerides - metabolism</topic><topic>Tumors</topic><topic>Urea - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VISEK, W. J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cancer research (Baltimore)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VISEK, W. J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitrogen-stimulated orotic acid synthesis and nucleotide imbalance</atitle><jtitle>Cancer research (Baltimore)</jtitle><addtitle>Cancer Res</addtitle><date>1992-04-01</date><risdate>1992</risdate><volume>52</volume><issue>7</issue><spage>2082s</spage><epage>2084s</epage><pages>2082s-2084s</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Orotic acid, first discovered in ruminant milk, is an intermediate in the pyrimidine biosynthesis pathway of animal cells. Its synthesis is initiated by the formation of carbamoyl phosphate (CP) in the cytoplasm, with ammonia derived from glutamine. Ureotelic species also form CP in the first step of urea synthesis in liver mitochondria. For that, ammonia is derived from tissue fluid. When there is insufficient capacity for detoxifying the load of ammonia presented for urea synthesis, CP leaves the mitochondria and enters the pyrimidine pathway, where orotic acid biosynthesis is stimulated, orotic acid excretion in urine then increases. Orotic acid synthesis is abnormally high with hereditary deficiencies of urea-cycle enzymes or uridine monophosphate synthase. It is also elevated by ammonia intoxication and during feeding of diets high in protein, high in lysine with respect to arginine, or deficient in arginine, ornithine, and citrulline. Rats fed 1% orotic acid or diets deficient in urea-cycle amino acids develop fatty livers, which has not been demonstrated in other species. Humans consuming 6 g of orotic acid daily have not shown adverse effects. Rats fed 1% orotic acid or arginine-deficient diets also showed more and larger foci positive for gamma-glutamyl transpeptidase and more liver tumors after administration of carcinogens and partial hepatectomy. Orotic acid feeding was also associated with the tendency for development of larger mammary tumors induced by chemical carcinogens in rats and with development of urinary bladder calculi containing high concentrations of orotic acid in mice. Conditions that raise tissue orotic acid change purine-pyrimidine ratios. It is unknown whether tissue orotate concentrations play a role in the recently observed enhanced proliferation of cells in the colon of rats fed high-protein, high-fat diets or in the promotion of chemically induced colon cancer by intrarectal administration of ammonium acetate.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>1544144</pmid></addata></record> |
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subjects | Ammonia - metabolism Animals Biological and medical sciences Carbamyl Phosphate - metabolism Carcinogenesis, carcinogens and anticarcinogens Cattle Chemical agents Humans Liver Neoplasms - chemically induced Medical sciences Milk - metabolism Orotic Acid - metabolism Orotic Acid - pharmacology Orotic Acid - urine Pyrimidines - biosynthesis Rats Triglycerides - metabolism Tumors Urea - metabolism |
title | Nitrogen-stimulated orotic acid synthesis and nucleotide imbalance |
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